NDC 46708-343

CANDESARTAN CILEXETIL

Candesartan Cilexetil

CANDESARTAN CILEXETIL is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Alembic Pharmaceuticals Limited. The primary component is Candesartan Cilexetil.

Product ID46708-343_5aa0e0cf-ac92-4c44-a0e5-8b16913fbd1a
NDC46708-343
Product TypeHuman Prescription Drug
Proprietary NameCANDESARTAN CILEXETIL
Generic NameCandesartan Cilexetil
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2018-12-05
Marketing CategoryANDA / ANDA
Application NumberANDA210302
Labeler NameAlembic Pharmaceuticals Limited
Substance NameCANDESARTAN CILEXETIL
Active Ingredient Strength16 mg/1
Pharm ClassesAngiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 46708-343-30

30 TABLET in 1 BOTTLE (46708-343-30)
Marketing Start Date2018-12-05
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 46708-343-30 [46708034330]

CANDESARTAN CILEXETIL TABLET
Marketing CategoryANDA
Application NumberANDA210302
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-12-05

NDC 46708-343-91 [46708034391]

CANDESARTAN CILEXETIL TABLET
Marketing CategoryANDA
Application NumberANDA210302
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-12-05

NDC 46708-343-90 [46708034390]

CANDESARTAN CILEXETIL TABLET
Marketing CategoryANDA
Application NumberANDA210302
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-12-05

Drug Details

Active Ingredients

IngredientStrength
CANDESARTAN CILEXETIL16 mg/1

OpenFDA Data

SPL SET ID:d5b43fa0-6678-4219-99f1-10d273d49baf
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 577776
  • 153823
  • 153822
    • UPC Code
  • 0346708342302
  • 0346708341305
  • 0346708343309

    • Pharmacological Class

    • Angiotensin 2 Receptor Antagonists [MoA]
    • Angiotensin 2 Receptor Blocker [EPC]

    NDC Crossover Matching brand name "CANDESARTAN CILEXETIL" or generic name "Candesartan Cilexetil"

    NDCBrand NameGeneric Name
    0378-3224candesartan cilexetilcandesartan cilexetil
    0378-3225candesartan cilexetilcandesartan cilexetil
    0378-3231candesartan cilexetilcandesartan cilexetil
    0378-3232candesartan cilexetilcandesartan cilexetil
    0781-5936Candesartan cilexetilCandesartan cilexetil
    0781-5937Candesartan cilexetilCandesartan cilexetil
    0781-5938Candesartan cilexetilCandesartan cilexetil
    0781-5939Candesartan cilexetilCandesartan cilexetil
    46708-060CANDESARTAN CILEXETILCANDESARTAN CILEXETIL
    46708-341CANDESARTAN CILEXETILCANDESARTAN CILEXETIL
    46708-342CANDESARTAN CILEXETILCANDESARTAN CILEXETIL
    46708-343CANDESARTAN CILEXETILCANDESARTAN CILEXETIL
    49884-658Candesartan cilexetilCandesartan cilexetil
    49884-659Candesartan cilexetilCandesartan cilexetil
    49884-660Candesartan cilexetilCandesartan cilexetil
    49884-661Candesartan cilexetilCandesartan cilexetil
    60687-119Candesartan cilexetilCandesartan cilexetil
    60687-130Candesartan cilexetilCandesartan cilexetil
    60687-241Candesartan cilexetilCandesartan cilexetil
    68151-3838Candesartan cilexetilCandesartan cilexetil
    68382-191Candesartan cilexetilCandesartan cilexetil
    68382-193Candesartan cilexetilCandesartan cilexetil
    68382-192Candesartan cilexetilCandesartan cilexetil
    68382-190Candesartan cilexetilCandesartan cilexetil
    70771-1206Candesartan cilexetilCandesartan cilexetil
    70771-1207Candesartan cilexetilCandesartan cilexetil
    70771-1204Candesartan cilexetilCandesartan cilexetil
    70771-1205Candesartan cilexetilCandesartan cilexetil
    62332-342CANDESARTAN CILEXETILCANDESARTAN CILEXETIL
    62332-341CANDESARTAN CILEXETILCANDESARTAN CILEXETIL
    62332-343CANDESARTAN CILEXETILCANDESARTAN CILEXETIL
    62332-060CANDESARTAN CILEXETILCANDESARTAN CILEXETIL
    0186-0004ATACANDCandesartan cilexetil
    0186-0008ATACANDCandesartan cilexetil
    0186-0016ATACANDCandesartan cilexetil
    0186-0032ATACANDCandesartan cilexetil
    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.